ClinVar Miner

Submissions for variant NM_000116.5(TAFAZZIN):c.207C>G (p.His69Gln)

dbSNP: rs1557191125
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV000676907 SCV000802722 pathogenic not provided 2016-03-04 no assertion criteria provided clinical testing

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